Glass composition for crystallized glass

ABSTRACT

A polished glass disk medium substrate suitable for use as a substrate for a hard disk, a hard disk containing the substrate and methods for making the substrate. The substrate containing glass forming raw materials may be formed so as to have a Young&#39;s modulus of 110 or higher.

RELATED APPLICATION

This application claims priority to Japanese Patent Application No. 2000-100817 filed in Japan on Apr. 3, 2000, the contents of which are hereby incorporated by reference.

1. Field of the Invention

The present invention relates to a glass composition, and specifically relates to a glass composition suited for crystallized glass. More specifically, the present invention relates to a composition for crystallized glass disk medium. Such disk medium include hard disks, magnetic disks, optical disks and magnetic-optical disks

2. Description of the Prior Art

Aluminum and glass are known materials suitable for use as magnetic disk substrates. Among these substrates, glass substrates have been the focus of most attention due to their superior surface smoothness and mechanical strength. Such glass substrates include chemically reinforced glass substrates strengthened by ion exchange on the surface, and crystallized glass substrates having strengthened bonds by depositing a crystal component on the substrate.

The performance demands of recent substrates have become more severe day by day, and improved performance is particularly sought regarding strength, flex and warp during high-speed rotation. This type of performance can be expressed by the Young's modulus of the substrate material, in which a higher numerical value is desirable.

For example, the composition disclosed in Japanese Laid-Open Patent Application No. 11-322362 attains a Young's modulus value of 130 or greater. However, this prior art requires extremely high thermal processing temperatures which complicate the manufacturing process, that is, this art requires a primary processing temperature of 800° C., and a secondary processing temperature of 1,000° C.

SUMMARY OF THE INVENTION

An object of the present invention is to provide an improved glass composition.

Another object of the present invention is to provide a glass composition having a high Young's modulus and which is highly suited for mass production.

These objects are attained with a glass composition of the present invention desirably having the main components within the ranges described below:

about 45 wt % or more, but less than about 60 wt % SiO₂;

about 5 wt % or more, but less than about 20 wt % Al₂O₃;

about 9 wt % or more, but less than about 25 wt % MgO;

about 0.1 wt % or more, but less than about 12 wt % TiO₂;

about 0.1 wt % or more, but less than about 12 wt % Li₂O; and

about 5 wt % or more, but less than about 22 wt % ZnO.

DESCRIPTION OF THE PREFERRED EMBODIMENT

The preferred embodiments of the present invention are described hereinafter.

These objects are attained with a glass composition of the present invention desirably having the main components within the ranges described below:

about 45 wt % or more, but less than about 60 wt % SiO₂;

about 5 wt % or more, but less than about 20 wt % Al₂O₃;

about 9 wt % or more, but less than about 25 wt % MgO;

about 0.1 wt % or more, but less than about 12 wt % TiO₂;

about 0.1 wt % or more, but less than about 12 wt % Li₂O; and

about 5 wt % or more, but less than about 22 wt % ZnO.

When the composition content of SiO₂ used as a glass forming oxide is less than about 45 wt %, melting characteristics are typically adversely affected, and when the percentage exceeds about 60 wt %, a stabilized state of glass is achieved and crystal deposition typically becomes difficult.

Aluminum oxide (Al₂O₃) is an intermediate oxide of glass, and is a structural component of the crystal-phase magnesium-aluminum crystals formed during heating. When the composition content is less than about 5 wt %, there are typically few crystals formed, and the desired strength is not obtained, whereas when the percentage exceeds about 20 wt %, the melting temperature is typically raised and devitrification readily occurs.

Magnesium oxide (MgO) is a fluxing agent, which is added to induce the crystal particles to nucleate and form crystal particle clusters. When the composition content is less than about 9 wt %, the working temperature range is typically narrowed, and the chemical durability of the glass matrix phase is not typically improved. When the composition content exceeds about 25 wt %, other crystal phase matter is often deposited and the desired strength is typically difficult to obtain.

Titanium oxide (TiO₂) is a crystal nucleating agent, which is often an essential component for magnesium silicate crystal deposition. Furthermore, TiO₂ functions as a fluxing agent to improve stability during production. When the composition content is less than about 0.1 wt %, melting characteristics are typically adversely affected, and crystal growth is often difficult. When the content exceeds about 12 wt %, crystallization typically progresses rapidly, the crystallization state often becomes difficult to control, the deposited crystals are typically coarse with heterogeneity of the crystal phase, and a fine homogeneous crystal structure often cannot be obtained, such that the required surface smoothness for use as a disk substrate is difficult to obtain by a polishing process. Furthermore, devitrification readily occurs during fusion molding, and mass production characteristics are reduced.

Stability during manufacture is improved by the addition of Li₂O, which functions as a fluxing agent. When the composition content is less than about 0.1 wt %, there is inadequate improvement in melting characteristics. When the composition content exceeds about 12 wt %, stability often decreases during the polishing and washing processes.

Zinc oxide (ZnO) functions as a fluxing agent which augments uniform crystal deposition. When the composition content is less than about 5 wt %, there is typically insufficient improvement in crystal homogeneity. When the composition content exceeds about 22 wt %, the glass becomes stable, and crystallization is suppressed, such that the desired strength is often difficult to obtain.

The manufacturing method is described below. The raw materials of the ultimately produced glass substrate are thoroughly mixed in specific proportions, then introduced to a platinum crucible and melted. After melting, the melted material is poured into a mold to form an approximate shape. Then the material is annealed to room temperature. Next, the material is maintained at a primary heating process temperature of about 500 to about 680° C. during a primary process (heating process) to generate crystal nuclei. Then, the material is maintained at a secondary heating process temperature of about 680 to about 800° C. during a secondary process to grow crystal nuclei. Then the material is cooled to obtain the crystallized glass.

This material may be used as a disk substrate by processing such as polishing to attain a desired shape and thickness.

By using the above raw materials and the process described herein, an extremely high Young's modulus and high mass production characteristics are obtainable. Even higher performance is obtained by adding the components described below in a suitable range.

Phosphoric anhydride (P₂O₅), which functions as a fluxing agent, is a nucleating agent for depositing silicate crystals, and is an important component for uniform deposition of crystals on the entirety of the glass. When the composition content is less than about 0.1 wt %, sufficient formation of crystal nuclei typically becomes difficult, crystal particles are often coarse, heterogeneous crystal deposition often occurs, the desired fine homogeneous crystal structure may be difficult to obtain, such that the required surface smoothness for use as a disk substrate may be difficult to obtain by a polishing process. When the content exceeds about 5.0 wt %, reactivity to the filter medium increases during melting, and devitrification increases so as to reduce mass production characteristics during fusion molding. Chemical durability typically decreases, there is concern that the magnetic layer may be affected, and stability is often reduced during the polishing and washing processes.

Adding ZrO₂ which functions as a glass modifying oxidant also functions effectively as a glass crystal nucleating agent. When the content ratio is less than about 0.1 wt %, sufficient formation of crystal nuclei typically becomes difficult, crystal particles are often coarse, heterogeneous crystal deposition often occurs, the desired fine homogeneous crystal structure may be difficult to obtain, such that the required surface smoothness for use as a disk substrate may be difficult to obtain by a polishing process. Furthermore, chemical durability and migration resistance are often reduced, there is concern that the magnetic layer may be affected, and stability is often reduced during the polishing and washing processes. When the content exceeds about 12 wt %, the melting temperature is raised, devitrification readily occurs, and fusion molding typically becomes difficult. Furthermore, the deposition crystal phase fluctuates such that desired characteristics are often difficult to obtain.

The addition of CaO, which functions as a fluxing agent, supplements uniform crystal deposition. When the composition content is less than about 0.1 wt %, sufficient improvement in crystal homogeneity is not typically obtained. When the content exceeds about 9 wt %, chemical durability is not typically improved.

Crystal nucleating material is increased by the addition of Nb₂O₅, which works as a fluxing agent. When the composition content is less than about 0.1 wt %, there is often inadequate rigidity improvement. When the composition content exceeds about 9 wt %, crystallization of the glass typically becomes unstable, the deposition crystal phase typically becomes uncontrollable, and the desired characteristics are often difficult to obtain.

The addition of Ta₂O₅, which works as a fluxing agent, improves fusion and strength, and also improves chemical durability in the glass matrix phase. When the composition content is less than about 0.1 wt %, there is typically inadequate rigidity improvement. When the composition content exceeds about 9 wt %, crystallization of the glass typically becomes unstable, the deposition crystal phase becomes uncontrollable, and the desired characteristics are often difficult to obtain.

Stability during manufacture is improved by the addition of K₂O, which functions as a fluxing agent. When the composition content is less than about 0.1 wt %, there is inadequate improvement in melting characteristics. When the composition content exceeds about 9 wt %, the glass typically becomes stable and crystallization is suppressed, chemical durability is often reduced, and there is concern that the magnetic layer will be affected, and stability often decreases during the polishing and washing processes.

Glass phase splitting is promoted by adding B₂O₃, which works as a former, and accelerates crystal deposition and growth. When the composition content is less than about 0.1 wt %, improvement of melting characteristics is typically inadequate. When the composition content exceeds about 9 wt %, glass devitrification readily occurs, molding typically becomes difficult, and the crystals often become coarse such that fine crystals is difficult to obtain.

Rigidity is improved by adding Y₂O₃, which functions as a fluxing agent. When the composition content is less than about 0.1 wt %, there is typically inadequate rigidity improvement. When the composition content exceeds about 9 wt %, crystal deposition is often suppressed, sufficient crystallization is difficult to obtain, and desired characteristics are often not attained.

Stability during mass production is improved by adding Sb₂O₃, which functions as a clarifier. When the composition content is less than about 0.1 wt %, there is typically insufficient clarification effect, and production characteristics are typically reduced. When the composition content exceeds about 9 wt %, crystallization of the glass often becomes unstable, the deposition crystal phase typically becomes uncontrollable, and the desired characteristics are often difficult to obtain.

Stability during production is improved by adding As₂O₃, which functions as a clarifier. When the composition content is less than about 0.1 wt %, there is often insufficient clarification effect, and production characteristics are often reduced. When the composition content exceeds about 9 wt %, crystallization of the glass typically becomes unstable, the deposition crystal phase typically becomes uncontrollable, and the desired characteristics are often difficult to obtain.

The glasses of the present invention may have one or more crystalline phases and an amorphous phase. The crystalline phases represent about 50 to about 60 percent of the total glass composition. Preferred embodiments include a main crystalline phase of clinoenstatite which desirably represents at least about 80 percent by weight of the total of all crystalline phases. Preferred embodiments may also include a secondary crystalline phase of, for example, enstatite magnesium aluminum silicate, and/or zinc titanium oxide which desirably represents less than about 20 percent by weight of the total crystalline phase.

Although the present invention is described in detail in the following examples, the invention is not limited to these examples. Tables 1-4 show the glass composition in percent-by-weight of Examples 1-40. Glass substrates were obtained by the previously described manufacturing method in accordance with these numerical examples.

In the tables, C1 represents a crystal phase of clinoenstatite (MgSiO₃), C2 represents a crystal phase of enstatite (MgSiO₃), M1 represents a crystal phase of magnesium aluminum silicate {(Mg Al)SiO₃}, Z1 represents a crystal phase of zinc titanium oxide (Zn₂Ti₃O₈) and Z2 represents a crystal phase of zinc titanium oxide (Zn₂TiO₄).

TABLE 1 Ex. 01 Ex. 02 Ex. 03 Ex. 04 Ex. 05 Ex. 06 Ex. 07 Ex. 08 Ex. 09 Ex. 10 SiO₂ 54.0 54.0 54.0 54.0 54.0 54.0 54.0 54.0 58.0 56.0 Al₂O₃ 9.0 13.5 18.0 17.1 10.0 9.0 5.0 5.0 10.0 12.0 MgO 13.5 13.5 9.0 13.5 15.0 9.0 22.0 9.0 23.5 20 TiO₂ 7.5 7.5 7.5 7.5 7.5 7.5 7.5 7.5 3.0 3.0 Li₂O 2.5 2.5 2.5 2.5 2.5 2.5 2.5 2.5 0.5 2.0 ZnO 13.1 8.6 8.6 5 10.6 17.6 8.6 21.6 5.0 7.0 Sb₂O₃ 0.4 0.4 0.4 0.4 0.4 0.4 0.4 0.4 Primary Treatment Temperature (° C.) 660 660 660 660 660 660 660 660 660 660 Secondary Treatment Temperature (° C.) 700 700 700 700 700 700 700 700 700 700 Primary Treatment Time (hr) 5 5 5 5 5 5 5 5 5 5 Secondary Treatment Temperature (hr) 5 5 5 5 5 5 5 5 5 5 Young's Modules (G Pa) 121 131 115 128 135 122 140 118 119 115 Diameter of Crystal (nm) 30 30 30 30 30 30 30 30 30 30 Main Crystal Phase C1 C1 C1 C1 C1 C1 C1 C1 C1 C1 Secondary Crystal Phase C2 C2 C2 C2 C2 C2 C2 C2 C2 C2 Other Crystal Phase M1 M1 M1 M1 M1 M1 M1 M1 M1 M1 Other Crystal Phase Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Other Crystal Phase Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2

TABLE 2 Ex. 11 Ex. 12 Ex. 13 Ex. 14 Ex. 15 Ex. 16 Ex 17 Ex. 18 Ex. 19 Ex. 20 SiO₂ 45.0 46.0 46.0 48.0 48.0 48.0 53.5 55.0 48.0 48.0 Al₂O₃ 8.0 14.0 8.0 15.0 15.0 15.0 15.0 15.0 18.0 15.0 MgO 20.0 20.0 23.0 10.0 10.0 8.0 12.0 8.0 17.0 12.0 TiO₂ 5.0 4.0 4.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 Li₂O 2.0 4.0 4.0 4.0 2.0 2.0 6.0 2.0 2.0 2.0 ZnO 10.0 12.0 15.0 18.0 20.0 22.0 8.0 12.0 8.0 12.0 P₂O₅ 0.5 3.0 ZrO₂ 2.0 6.0 Primary Treatment Temperature (° C.) 660 660 660 660 660 660 660 660 660 660 Secondary Treatment Temperature (° C.) 700 700 700 700 700 700 700 700 700 700 Primary Treatment Time (hr) 5 5 5 5 5 5 5 5 5 5 Secondary Treatment Temperature (hr) 5 5 5 5 5 5 5 5 5 5 Young's Modules (G Pa) 122 116 115 115 110 110 110 112 114 113 Diameter of Crystal (nm) 30 30 30 30 30 30 30 30 30 30 Main Crystal Phase C1 C1 C1 C1 C1 C1 C1 C1 C1 C1 Secondary Crystal Phase C2 C2 C2 C2 C2 C2 C2 C2 C2 C2 Other Crystal Phase M1 M1 M1 M1 M1 M1 M1 M1 M1 M1 Other Crystal Phase Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Other Crystal Phase Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2

TABLE 3 Ex. 21 Ex. 22 Ex. 23 Ex. 24 Ex. 25 Ex. 26 Ex. 27 Ex. 28 Ex. 29 Ex. 30 SiO₂ 48.0 48.0 48.0 48.0 48.0 48.0 48.0 48.0 48.0 48.0 Al₂O₃ 15.0 15.0 15.0 15.0 15.0 15.0 15.0 15.0 15.0 19.0 MgO 15.0 8.0 20.0 13.0 20.0 13.0 22.0 14.0 13.0 8.0 TiO₂ 10.0 9.0 5.0 5.0 5.0 5.0 5.0 5.0 10.0 5.0 Li₂O 2.0 2.0 2.0 2.0 2.0 2.0 2.0 2.0 4.0 2.0 ZnO 8.0 12.0 8.0 12.0 8.0 12.0 7.8 12.0 8.0 12.0 CaO 2.0 6.0 Nb₂O₅ 2.0 5.0 Ta₂O₅ 2.0 5.0 K₂O 0.2 4.0 B₂O₃ 2.0 6.0 Primary Treatment Temperature (° C.) 660 660 660 660 660 660 660 660 660 660 Secondary Treatment Temperature (° C.) 700 700 700 700 700 700 700 700 700 700 Primary Treatment Time (hr) 5 5 5 5 5 5 5 5 5 5 Secondary Treatment Temperature (hr) 5 5 5 5 5 5 5 5 5 5 Young's Modules (G Pa) 146 135 117 114 115 113 117 112 143 112 Diameter of Crystal (nm) 30 30 30 30 30 30 30 30 30 30 Main Crystal Phase C1 C1 C1 C1 C1 C1 C1 C1 C1 C1 Secondary Crystal Phase C2 C2 C2 C2 C2 C2 C2 C2 C2 C2 Other Crystal Phase M1 M1 M1 M1 M1 M1 M1 M1 M1 M1 Other Crystal Phase Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Other Crystal Phase Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2

TABLE 4 Ex. 31 Ex. 32 Ex. 33 Ex. 34 Ex. 35 Ex. 36 Ex. 37 Ex. 38 Ex. 39 Ex. 40 SiO₂ 55.0 54.0 58.0 57.5 60.0 54.0 57.0 50.0 60.0 53.0 Al₂O₃ 15.0 15.0 15.0 15.0 15.0 15.0 15.0 15.0 15.0 15.0 MgO 13.0 8.0 11.8 8.0 8.0 8.0 8.0 8.0 8.0 8.0 TiO₂ 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 Li₂O 2.0 2.0 2.0 2.0 2.0 2.0 2.0 2.0 2.0 2.0 ZnO 8.0 12.0 8.0 12.0 8.0 12.0 8.0 12.0 8.0 12.0 Y₂O₃ 2.0 4.0 Sb₂O₃ 0.2 0.5 2.0 4.0 5.0 8.0 As₂O₃ 2.0 5.0 Primary Treatment Temperature (° C.) 660 660 660 660 660 660 660 660 660 660 Secondary Treatment Temperature (° C.) 700 700 700 700 700 700 700 700 700 700 Primary Treatment Time (hr) 5 5 5 5 5 5 5 5 5 5 Secondary Treatment Temperature (hr) 5 5 5 5 5 5 5 5 5 5 Young's Modules (G Pa) 116 112 114 112 113 112 112 113 114 115 Diameter of Crystal (nm) 30 30 30 30 30 30 30 30 30 30 Main Crystal Phase C1 C1 C1 C1 C1 C1 C1 C1 C1 C1 Secondary Crystal Phase C2 C2 C2 C2 C2 C2 C2 C2 C2 C2 Other Crystal Phase M1 M1 M1 M1 M1 M1 M1 M1 M1 M1 Other Crystal Phase Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Z1 Other Crystal Phase Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2 Z2

The present invention provides a glass substrate having excellent production characteristics and a Young's modulus of 110 or higher.

Although the present invention has been fully described by way of examples with reference to the accompanying drawings, it is to be noted that various changes and modification will be apparent to those skilled in the art. Therefore, unless such changes and modifications depart from the scope of the present invention, they should be construed as being included therein. 

What is claimed is:
 1. A polished glass ceramic disk medium substrate comprising crystalline and amorphous phases formed of a mixture of glass forming raw materials comprising about 45% to about 60% by weight SiO₂; about 5% to about 20% by weight Al₂O₃; about 9% to about 25% by weight MgO; about 0.1% to about 12% by weight TiO₂; about 0.1% to about 12% by weight Li₂O; and about 5% to about 22% by weight ZnO, wherein said glass substrate has a Young's modulus of 110 GPa or higher.
 2. The polished glass ceramic disk medium substrate according to claim 1, wherein the raw materials further comprise about 0.1% to about 5% by weight P₂O₅.
 3. The polished glass ceramic disk medium substrate according to claim 1, wherein the raw materials further comprise about 0.1% to about 12% by weight ZrO₂.
 4. The polished glass ceramic disk medium substrate according to claim 1, wherein the raw materials further comprise about 0.1% to about 9% by weight CaO.
 5. The polished glass ceramic disk medium substrate according to claim 1, wherein the raw materials further comprise about 0.1% to about 9% by weight Nb₂O₅.
 6. The polished glass ceramic disk medium substrate according to claim 1, wherein the raw materials further comprise about 0.1% to about 9% by weight Ta₂O₅.
 7. The polished glass ceramic disk medium substrate according to claim 1, wherein the raw materials further comprise about 0.1% to about 9% by weight K₂O.
 8. The polished glass ceramic disk medium substrate according to claim 1, wherein the raw materials further comprise about 0.1% to about 9% by weight B₂O₃.
 9. The polished glass ceramic disk medium substrate according to claim 1, wherein the raw materials further comprise about 0.1% to about 9% by weight Y₂O₃.
 10. The polished glass ceramic disk medium substrate according to claim 1, wherein the raw materials further comprise about 0.1% to about 9% by weight Sb₂O₃.
 11. The polished glass ceramic disk medium substrate according to claim 1, wherein the raw materials further comprise about 0.1% to about 9% by weight As₂O₃.
 12. The polished glass ceramic disk medium substrate according to claim 1, said raw materials consisting essentially of about 45% to about 60% by weight SiO₂; about 5% to about 20% by weight Al₂O₃; about 9% to about 25% by weight MgO; about 0.1% to about 12% by weight TiO₂; about 0.1% to about 12% by weight Li₂O; and about 5% to about 22% by weight ZnO.
 13. The polished glass ceramic disk medium substrate according to claim 12, further containing one or more of the following: about 0.1% to about 5% by weight P₂O₅; about 0.1% to about 12% by weight ZrO₂; about 0.1% to about 9% by weight CaO; about 0.1% to about 9% by weight Nb₂O₅; about 0.1% to about 9% by weight Ta₂O₅; about 0.1% to about 9% by weight K₂O; about 0.1% to about 9% by weight B₂O₃; about 0.1% to about 9% by weight Y₂O₃; about 0.1% to about 9% by weight Sb₂O₃; and about 0.1% to about 9% by weight As₂O₃.
 14. The polished glass ceramic disk medium substrate according to claim 12, wherein said substrate is essentially free of BaO, ZrO₂, B₂O₃ and NiO.
 15. The polished glass ceramic disk medium substrate according to claim 1, wherein the crystalline phases represent about 50 to about 60 percent by weight of the total glass composition.
 16. The polished glass ceramic disk medium substrate according to claim 1, comprising a crystalline phase of clinoenstatite.
 17. The polished glass ceramic disk medium substrate according to claim 16, wherein the crystalline phase of clinoenstatite represents at least about 80 percent by weight of the crystalline phases.
 18. The polished glass ceramic disk medium substrate according to claim 1, comprising a crystalline phase of enstatite.
 19. The polished glass ceramic disk medium substrate according to claim 18, wherein the crystalline phase of enstatite represents less than or equal to about 20 percent by weight of the crystalline phases.
 20. The polished glass ceramic disk medium substrate according to claim 1, comprising a crystalline phase of magnesium aluminum silicate.
 21. The polished glass ceramic disk medium substrate according to claim 20, wherein the crystalline phase of magnesium aluminum silicate represents less than or equal to about 20 percent by weight of the crystalline phases.
 22. The polished glass ceramic disk medium substrate according to claim 1, comprising a crystalline phase of Zn₂Ti₃O₈.
 23. The polished glass ceramic disk medium substrate according to claim 22, wherein the crystalline phase of Zn₂Ti₃O₈ represents less than or equal to about 20 percent by weight of the crystalline phases.
 24. The polished glass ceramic disk medium substrate according to claim 1, comprising a crystalline phase of Zn₂TiO₄.
 25. The polished glass ceramic disk medium substrate according to claim 24, wherein the crystalline phase of Zn₂TiO₄ represents less than or equal to about 20 percent by weight of the crystalline phase.
 26. The polished glass ceramic disk medium substrate according to claim 1, comprising a main crystalline phase of clinoenstatite and a secondary crystalline phase of enstatite.
 27. The polished glass ceramic disk medium substrate according to claim 26, further comprising one or more of a crystalline phase of magnesium aluminum silicate, a crystalline phase of Zn₂Ti₃O₈ and a crystalline phase of Zn₂TiO₄.
 28. The polished glass ceramic disk medium substrate according to claim 1, wherein said substrate is prepared by heating glass forming raw materials to a temperature, T₁, between about 500 and 680° C. to generate crystal nuclei; heating at a temperature, T₂, between about 680 and about 800° C. to grow crystal nuclei; and cooling to obtain crystallized glass.
 29. A recording disk comprising the polished glass ceramic disk medium substrate defined in claim
 1. 30. The recording disk according to claim 29, wherein said recording disk is a hard disk.
 31. The recording disk according to claim 29, wherein said recording disk is a magnetic disk.
 32. The recording disk according to claim 29, wherein said recording disk is an optical disk.
 33. The recording disk according to claim 29, wherein said recording disk is a magnetic-optical disk.
 34. A method of making a glass ceramic disk medium substrate comprising: heating glass forming raw materials to a temperature sufficiently high to melt the raw materials: forming a disk medium substrate; and crystallizing the disk medium substrate, wherein said crystallizing comprises heating the disk medium substrate to a temperature, T₁, between about 500 and 680° C. to generate crystal nuclei; heating at a temperature, T₂, between about 680 and about 800° C. to grow crystal nuclei; and cooling to obtain crystallized glass, wherein the glass forming raw materials comprise about 45% to about 60% by weight SiO₂; about 5% to about 20% by weight Al₂O₃; about 9% to about 25% by weight MgO; about 0.1% about 12% by weight TiO₂; about 0.1% to about 12% by weight Li₂O; and about 5% to about 22% by weight ZnO, wherein said glass substrate has a Young's modulus of 110 GPa or higher.
 35. The method according to claim 34, further comprising polishing said glass ceramic disk medium substrate. 